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HADH antibody

The Rabbit Polyclonal anti-HADH antibody (ABIN7003627) specifically detects HADH in WB and ELISA. The antibody is reactive with Human, Mouse and Rat samples.
Catalog No. ABIN7003627
-15% Promotion 2026
$121.38
$142.80
save $21.42 (-15 %)
Plus shipping costs $50.00
20 μL
Shipping to: United States
Delivery in 11 to 14 Business Days

Quick Overview for HADH antibody (ABIN7003627)

Target

See all HADH Antibodies
HADH (Hydroxyacyl-CoA Dehydrogenase (HADH))

Reactivity

  • 40
  • 38
  • 23
  • 8
  • 5
  • 3
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 1
Human, Mouse, Rat

Host

  • 40
  • 15
  • 1
  • 1
Rabbit

Clonality

  • 43
  • 14
Polyclonal

Conjugate

  • 28
  • 4
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This HADH antibody is un-conjugated

Application

  • 41
  • 14
  • 14
  • 14
  • 13
  • 10
  • 9
  • 9
  • 6
  • 3
  • 2
  • 2
  • 2
  • 2
  • 1
Western Blotting (WB), ELISA
  • Characteristics

    Polyclonal Antibody

    Purification

    Antigen affinity purification

    Immunogen

    Synthetic peptide of human HADH

    Isotype

    IgG
  • Application Notes

    WB 1:500-1:2000, ELISA 1:5000-1:10000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.6 mg/mL

    Buffer

    PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4

    Preservative

    Sodium azide

    Precaution of Use

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Storage

    -20 °C

    Storage Comment

    Store at -20°C. Avoid freeze / thaw cycles.
  • Target

    HADH (Hydroxyacyl-CoA Dehydrogenase (HADH))

    Alternative Name

    HADH

    Background

    This gene is a member of the 3-hydroxyacyl-CoA dehydrogenase gene family. The encoded protein functions in the mitochondrial matrix to catalyze the oxidation of straight-chain 3-hydroxyacyl-CoAs as part of the beta-oxidation pathway. Its enzymatic activity is highest with medium-chain-length fatty acids. Mutations in this gene cause one form of familial hyperinsulinemic hypoglycemia. The human genome contains a related pseudogene of this gene on chromosome 15.

    Molecular Weight

    Observed_MW: Refer to figures

    Calculated_MW: 34 kDa

    UniProt

    Q16836

    Pathways

    Negative Regulation of Hormone Secretion, Monocarboxylic Acid Catabolic Process
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